Aladin ATANDI BATCHY, Luc Magloire Anicet Boumba, C. Elenga-Bongo, Ghislain LOUBANO VOUMBI, Freddy Saturnin Pouki, Fredy Kibouilou, Ange Malonga, D. Moukassa, M. Diatewa
{"title":"Human Cytomegalovirus Infection Associated with Low Insulin Secretion in a Type 1 Diabetic Population in Pointe Noire","authors":"Aladin ATANDI BATCHY, Luc Magloire Anicet Boumba, C. Elenga-Bongo, Ghislain LOUBANO VOUMBI, Freddy Saturnin Pouki, Fredy Kibouilou, Ange Malonga, D. Moukassa, M. Diatewa","doi":"10.52106/2766-3213.1040","DOIUrl":null,"url":null,"abstract":"Viral infections are one of the triggers and aggravators factors type 1 diabetes (T1D) development. Among these infections, human cytomegalovirus infection affects 60-90% of the world’s population. The aim of this study was to describe the metabolic consequences of Cytomegalovirus infection in T1D subjects. We conducted a descriptive cross-sectional study over 6 months between June and November 2021. A total of 72 T1D subjects were enrolled. The following laboratory tests were performed: fasting blood glucose, HbA1c, C peptide, lipid profile and CMV serology. The mean age of the patients was 19. 8±4.3 years with a sex ratio (M/F) of 1.4. CMV serology was positive in 75% of T1D patients. We noticed a disturbance of the biochemical markers in T1D+CMV+ patients. The homeostasis model of β-cell function (HOMA β) evaluation was significantly lower in T1D+CMV+ patients compared to T1D+CMV- patients. Blood glucose (8.69±5.30 vs 7.08±6.71 P=0.009), HbA1C (10.42±2.85 vs 8.77±2.90 P=0.009), TC (2.04±0.37 vs 1.97±0.28 P=0.0039), HDL-C (0.26±0.11 vs 0.19±0.007 P=0.0091), LDL-C (1.25±0.55 vs 1.20±0.50 P= 0.0039), were higher in T1D+CMV+ vs T1D+CMV-. However, creatinine (8.20±1.80 vs 9.13±1.07 P=0.0039), C peptide (0.15±0.003 vs 0.13±0.002 P=0.009) were higher in T1D+CMV- than in T1D+CMV+. The present study showed that CMV infection was associated with disturbed metabolic characteristics in T1D and deep insulin deficiency.","PeriodicalId":375458,"journal":{"name":"MEDICAL AND CLINICAL RESEARCH: OPEN ACCESS","volume":"31 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2022-06-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"MEDICAL AND CLINICAL RESEARCH: OPEN ACCESS","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.52106/2766-3213.1040","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Viral infections are one of the triggers and aggravators factors type 1 diabetes (T1D) development. Among these infections, human cytomegalovirus infection affects 60-90% of the world’s population. The aim of this study was to describe the metabolic consequences of Cytomegalovirus infection in T1D subjects. We conducted a descriptive cross-sectional study over 6 months between June and November 2021. A total of 72 T1D subjects were enrolled. The following laboratory tests were performed: fasting blood glucose, HbA1c, C peptide, lipid profile and CMV serology. The mean age of the patients was 19. 8±4.3 years with a sex ratio (M/F) of 1.4. CMV serology was positive in 75% of T1D patients. We noticed a disturbance of the biochemical markers in T1D+CMV+ patients. The homeostasis model of β-cell function (HOMA β) evaluation was significantly lower in T1D+CMV+ patients compared to T1D+CMV- patients. Blood glucose (8.69±5.30 vs 7.08±6.71 P=0.009), HbA1C (10.42±2.85 vs 8.77±2.90 P=0.009), TC (2.04±0.37 vs 1.97±0.28 P=0.0039), HDL-C (0.26±0.11 vs 0.19±0.007 P=0.0091), LDL-C (1.25±0.55 vs 1.20±0.50 P= 0.0039), were higher in T1D+CMV+ vs T1D+CMV-. However, creatinine (8.20±1.80 vs 9.13±1.07 P=0.0039), C peptide (0.15±0.003 vs 0.13±0.002 P=0.009) were higher in T1D+CMV- than in T1D+CMV+. The present study showed that CMV infection was associated with disturbed metabolic characteristics in T1D and deep insulin deficiency.
病毒感染是引发和加重1型糖尿病(T1D)发展的因素之一。在这些感染中,人类巨细胞病毒感染影响世界人口的60-90%。本研究的目的是描述巨细胞病毒感染在T1D受试者中的代谢后果。我们在2021年6月至11月期间进行了为期6个月的描述性横断面研究。共纳入72名T1D受试者。进行以下实验室检查:空腹血糖、糖化血红蛋白、C肽、血脂和巨细胞病毒血清学。患者的平均年龄为19岁。8±4.3岁,性别比(M/F) 1.4。75%的T1D患者CMV血清学阳性。我们注意到T1D+CMV+患者的生化标志物出现紊乱。与T1D+CMV-患者相比,T1D+CMV-患者的β细胞功能稳态模型(HOMA β)评估显着降低。血糖(8.69±5.30 vs 7.08±6.71 P=0.009)、HbA1C(10.42±2.85 vs 8.77±2.90 P=0.009)、TC(2.04±0.37 vs 1.97±0.28 P=0.0039)、HDL-C(0.26±0.11 vs 0.19±0.007 P=0.0091)、LDL-C(1.25±0.55 vs 1.20±0.50 P=0.0039)在T1D+CMV+组高于T1D+CMV-组。T1D+CMV-组肌酐(8.20±1.80 vs 9.13±1.07 P=0.0039)、C肽(0.15±0.003 vs 0.13±0.002 P=0.009)高于T1D+CMV+组。目前的研究表明,巨细胞病毒感染与T1D和深度胰岛素缺乏的代谢特征紊乱有关。